To gain an understanding of GCP in research and its practical application for studies involving patients or volunteers. The course covers the rationale for the GCP standards, study set up, essential documents, informed consent, site file management, adverse event reporting, data entry and audit expectations. This course is suitable for researchers undertaking Clinical Trials Involving Investigational Medicinal Products.
PLEASE NOTE – classroom training is required for all staff who have not previously completed GCP training. For people who have previously held a UHL/UoL/NIHR certificate, online training is available.
This session will be held in the professorial seminar room at Leicester General Hospital.